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1دورية أكاديمية
المصدر: BMC Ophthalmology, Vol 22, Iss 1, Pp 1-13 (2022)
مصطلحات موضوعية: Diabetic retinopathy, Inflammasome, Biomarkers, Vitreous, Serum, Cytokines, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1471-2415Test
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2دورية أكاديمية
المؤلفون: Anne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, C. Scott Gallagher, Tanya J. Major, Marilyn E. Merriman, Ruth K. Topless, Riku Takei, Nicola Dalbeth, Rinki Murphy, Lisa K. Stamp, Janak de Zoysa, Philip L. Wilcox, Keolu Fox, Kaja A. Wasik, Tony R. Merriman, Stephane E. Castel
المصدر: BMC Genomics, Vol 22, Iss 1, Pp 1-14 (2021)
مصطلحات موضوعية: Biotechnology, TP248.13-248.65, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1471-2164Test
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3دورية أكاديمية
المؤلفون: Zhanxuan E. Wu, Karl Fraser, Marlena C. Kruger, Ivana R. Sequeira, Wilson Yip, Louise W. Lu, Lindsay D. Plank, Rinki Murphy, Garth J. S. Cooper, Jean-Charles Martin, Sally D. Poppitt
المصدر: Nutrition & Metabolism, Vol 17, Iss 1, Pp 1-19 (2020)
مصطلحات موضوعية: Metabolomics, Type 2 diabetes, Visceral adiposity, Nutrition. Foods and food supply, TX341-641, Nutritional diseases. Deficiency diseases, RC620-627
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s12986-020-00518-zTest; https://doaj.org/toc/1743-7075Test
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4
المؤلفون: Rinki Murphy, Deborah J G Mackay, Ed A Mitchell
المصدر: BMC Medical Genetics, Vol 13, Iss 1, p 99 (2012)
BMC Medical Geneticsمصطلحات موضوعية: medicine.medical_specialty, lcsh:Internal medicine, Beckwith-Wiedemann Syndrome, Adolescent, lcsh:QH426-470, Beckwith–Wiedemann syndrome, Case Report, Biology, Genomic Imprinting, Internal medicine, Leukocytes, medicine, GNAS complex locus, Genetics, Humans, Insulin like growth factor 2 gene, Genetics(clinical), Multiplex ligation-dependent probe amplification, Imprinting (psychology), lcsh:RC31-1245, Genetics (clinical), Chromosomes, Human, Pair 11, Silver–Russell syndrome, Infant, Newborn, Mouth Mucosa, DNA, Small for gestational age, DNA Methylation, medicine.disease, Hypoglycemia, Silver-Russell Syndrome, lcsh:Genetics, Endocrinology, Beckwith Wiedemann syndrome, Infant, Small for Gestational Age, DNA methylation, biology.protein, Female, Genomic imprinting, Hernia, Umbilical
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd812c83a3e30e102e6856fb102f710Test
http://www.biomedcentral.com/1471-2350/13/99Test